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2,3-Dihydro-1H-indole-2-carboxamide → 2-Aminomethylindoline

HRID 1601076
ノート
印刷プレビュー

反応式

HRID 1601076 の反応式
[H-].[H-].[H-].[H-].[Li+].[Al+3].[NH:7]1[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH2:9][CH:8]1[C:16]([NH2:18])=O>C1COCC1>[NH2:18][CH2:16][CH:8]1[CH2:9][C:10]2[C:15](=[CH:14][CH:13]=[CH:12][CH:11]=2)[NH:7]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 139378102,3-Dihydro-1H-indole-2-carboxamideHCID 21226445Aluminium lithium hydride2 回

生成物 1

HCID 218304062-Aminomethylindoline収率 51%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

LAH (20 mL, 1M solution in THF) was added dropwise through a syringe to a solution of (±)-indoline-2-carboxamide (2.2 g, 13.6 mmol) in anhydrous THF (20 mL) with cooling, and the resulting solution was refluxed under argon for 5 h. More LAH (20 mL) was added, and reflux was continued for another 6 h. 10% aqueous THF was added dropwise with cooling to destroy excess LAH, and then Et2O was added. After stirring for 10 min, the colorless precipitate was removed by filtration and washed with THF. The filtrate was dried (K2CO3), concentrated, and purified by silica gel flash chromatography (90:10:0.2 CH2Cl2 /MeOH/Et3N). The title compound (1.02 g, 51%) was obtained as an amber oil: MS (ES) m/e 149.0 (M+H)+.

後処理

  1. temperaturewith cooling
  2. temperaturethe resulting solution was refluxed under argon for 5 h
  3. temperaturereflux
  4. temperaturewith cooling
  5. customto destroy excess LAH
  6. additionEt2O was added
  7. customthe colorless precipitate was removed by filtration
  8. washwashed with THF
  9. dry with materialThe filtrate was dried (K2CO3)
  10. concentrationconcentrated
  11. custompurified by silica gel flash chromatography (90:10:0.2 CH2Cl2 /MeOH/Et3N)

出典と根拠

ORDレコード
ord-1f0214d779e84795af0f569e1d3eee14
出典データセット
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05977101

反応ノート

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